Antiperspirant Deodorant Clean Powder 2oz

Manufacturer
China Ningbo Shangge Cosmetics Technology Corp.
Effective date
2026-01-05
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:31:15

Label at a glance#

ProductAntiperspirant Deodorant Clean Powder 2oz
Active ingredientALUMINUM CHLOROHYDRATE
Label structure11 sections

Dosage and administration

Remove cap. Turn dial to raise product. Apply evenly to underarm only. Replace cap after use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 19%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION


Reduces underarm wetness and perspiration.

Warnings

WARNINGS SECTION


For external use only

Do not use

OTC - DO NOT USE SECTION


Do not use on broken or irritated skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION


Stop use and ask a doctor if irritation or rash develops.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION


Ask a doctor before use if you have kidney disease.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION


Remove cap. Turn dial to raise product. Apply evenly to underarm only. Replace cap after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION


Mineral Oil
Cetearyl Alcohol
Talc
Cyclopentasiloxane
Isopropyl Myristate
Hydrogenated Castor Oil
Petrolatum
Corn Starch Modified
Fragrance
Sodium Bicarbonate

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiperspirant Deodorant Clean Powder 2ozAntiperspirant Deodorant Clean Powder 2oz

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130849607076588GTIN-13: 0849607076588
EAN-13: 0849607076588
GTIN-12: 849607076588
UPC-A: 849607076588
GTIN storage (14 digits): 00849607076588
Antiperspirant Deodorant Clean Powder 2oz.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58503-209-01Antiperspirant Deodorant Clean Powder 2oz57 g in 1 BOTTLEPOWDER576
58503-209-02Antiperspirant Deodorant Clean Powder 2oz45 g in 1 BOTTLEPOWDER456

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58503-20958503-209-01, 58503-209-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antiperspirant Deodorant Clean Powder 2ozALUMINUM CHLOROHYDRATE STICKChina Ningbo Shangge Cosmetics Technology Corp.479fd805-6fb5-7cdb-e063-6394a90a709e2026-01-05WarningsExact identifier
ndc (package): 58503-209-02
ndc (package): 58503-209-01
ndc (product): 58503-209
ndc11 (package): 58503020902
ndc11 (package): 58503020901
spl id: 479f7289-0b9a-07d3-e063-6394a90a26b4
spl set id: 479fd805-6fb5-7cdb-e063-6394a90a709e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.